Canonical Allele Identifier: PA2825161348
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2151387
ClinVar RCV Id: RCV003061316

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Thr310Pro
CA379962129
NM_000378.6:c.928A>C